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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384350Generated: October 26, 2026

Sodium Hydroxide → 6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinoline

https://huagongshe.com/reaction/1384350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
Reactant6-Bromo4-(3-ethoxy-phenyl)-1h-quinolin-2-oneHCID 22465443—
Solvent1,1-DichloroethaneHCID 6365—
Product6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinolineHCID 2246541958.2%

Reaction Steps

To a suspension of 6-bromo-4-(3-ethoxy-phenyl)-1H-quinolin-2-one (7.4 g, 21.5 mmol) in 60 ml dichloroethane was added trimethyloxonium tetrafluoroborate (BF4OMe3, 3.66 g, 24.7 mmol). The resulting mixture was stirred at ambient temperature overnight. After cooling to 0 C, was added 60 ml of 10% aqueous NaOH dropwise. The reaction mixture was stirred for another six hours at ambient temperature. It was then partitioned between dichloromethane and water. The organic layer was washed brine, dried over MgSO4, filtered and concentrated under vacuum to give an off-white solid. The solid was chromatographed on flash silica gel eluting with dichoromethane to yield the titled compound of 23A as a white solid (4.48 g, 58% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258824B1
Source datasetuspto-grants-2001_07
ORD IDord-fdb4f96527c44bb18d83c2294ca947f1
Source noteuspto-grants-2001_07